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CHINOLIN DERIVATIVES VEZÖGERN THE EFFECT OF GROWTH FACTORS SUCH AS VEGF

机译:胆碱类衍生物维泽根对生长因子如VEGF的影响

摘要

Compounds of the formula (I):wherein: R2 represents hydroxy, halogeno, C1-3alkyl, C1-3alkoxy, C1-3alkanoyloxy, trifluoromethyl, cyano, amino or nitro; n is an integer from 0 to 5; Z represents -O-, -NH-, -S- or -CH2-; G1 represents phenyl or a 5-10 membered heteroaromatic cyclic or bicyclic group; Y1, Y2, Y3 and Y4 each independently represents carbon or nitrogen; R1 represents fluoro or hydrogen; m is an integer from 1 to 3; R3 represents hydrogen, hydroxy, halogeno, cyano, nitro, trifluoromethyl, C1-3alkyl, -NR4R5 (wherein R4 and R5, can each be hydrogen or C1-3alkyl), or a group R6-X1- wherein X1 represents -CH2- or a heteroatom linker group and R6 is an alkyl, alkenyl or alkynyl chain optionally substituted by for example hydroxy, amino, nitro, alkyl, cycloalkyl, alkoxyalkyl, or an optionally substituted group selected from pyridone, phenyl and a heterocyclic ring, which alkyl, alkenyl or alkynyl chain may have a heteroatom linker group, or R6 is an optionally substituted group selected from pyridone, phenyl and a heterocyclic ring and salts thereof, in the manufacture of a medicament for use in the production of an antiangiogenic and/or vascular permeability reducing effect in warm-blooded animals such as humans, processes for the preparation of such derivatives, pharmaceutical compositions containing a compound of formula I or a pharmaceutically acceptable salt thereof as active ingredient and compounds of formula I. The compounds of formula I and the pharmaceutically acceptable salts thereof inhibit the effects of VEGF, a property of value in the treatment of a number of disease states including cancer and rheumatoid arthritis.
机译:式(I)的化合物:其中:R 2代表羟基,卤代,C 1-3烷基,C 1-3烷氧基,C 1-3烷酰氧基,三氟甲基,氰基,氨基或硝基; n是0至5的整数; Z代表-O-,-NH-,-S-或-CH 2-; G 1代表苯基或5-10元杂芳族环状或双环基团; Y 1,Y 2,Y 3和Y 4各自独立地表示碳或氮。 R 1代表氟或氢; m是1至3的整数; R 3代表氢,羟基,卤代,氰基,硝基,三氟甲基,C 1-3烷基,-NR 4 R 5(其中R 4和R 5各自可以是氢或C 1-3烷基)或基团R 6 -X 1-,其中X 1代表-CH 2-或杂原子连接基团,且R 6是任选被例如羟基,氨基取代的烷基,烯基或炔基链,硝基,烷基,环烷基,烷氧基烷基或选自吡啶酮,苯基和杂环的任选取代的基团,其中烷基,烯基或炔基链可具有杂原子连接基团,或R 6为选自以下的任选取代的基团吡啶酮,苯基和杂环及其盐,用于制造在温血动物(例如人)中产生抗血管生成和/或血管通透性降低作用的药物,此类衍生物的制备方法,药物含有式I化合物或其药学上可接受的盐作为活性成分的组合物式I化合物及其药学上可接受的盐抑制VEGF的作用,VEGF是治疗许多疾病包括癌症和类风湿性关节炎的有价值的特性。

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